NEUROMUSCULAR DISEASES
Ikerbasque, Fundación Vasca para la Ciencia
Bilbao, EspañaPublications in collaboration with researchers from Ikerbasque, Fundación Vasca para la Ciencia (33)
2024
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3D Neuronal Monitoring Platforms for Electrochemical Sensing Of Neurotransmitters
World Congress on Recent Advances in Nanotechnology
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Biallelic variants in SNUPN cause a limb girdle muscular dystrophy with myofibrillar-like features
Brain, Vol. 147, Núm. 8, pp. 2867-2883
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Dysregulated FOXO1 activity drives skeletal muscle intrinsic dysfunction in amyotrophic lateral sclerosis
Acta Neuropathologica, Vol. 148, Núm. 1
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Elevated cholesterol in ATAD3 mutants is a compensatory mechanism that leads to membrane cholesterol aggregation
Brain, Vol. 147, Núm. 5, pp. 1899-1913
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Understanding the olfactory role in post-COVID cognitive and neuropsychiatric manifestations
Frontiers in Psychology, Vol. 15
2023
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Dysautonomia and small fiber neuropathy in post-COVID condition and Chronic Fatigue Syndrome
Journal of Translational Medicine, Vol. 21, Núm. 1
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Pharmacokinetic Evaluation of New Drugs Using a Multi-Labelling Approach and PET Imaging: Application to a Drug Candidate with Potential Application in Neuromuscular Disorders
Biomedicines, Vol. 11, Núm. 2
2022
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Brain fog of post-COVID-19 condition and Chronic Fatigue Syndrome, same medical disorder?
Journal of Translational Medicine, Vol. 20, Núm. 1
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Defects of Nutrient Signaling and Autophagy in Neurodegeneration
Frontiers in Cell and Developmental Biology, Vol. 10
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Electroactive 3D printable poly(3,4-ethylenedioxythiophene)-: Graft -poly(ϵ-caprolactone) copolymers as scaffolds for muscle cell alignment
Polymer Chemistry, Vol. 13, Núm. 1, pp. 109-120
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Targeting Myotonic Dystrophy Type 1 with Metformin
International Journal of Molecular Sciences, Vol. 23, Núm. 5
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Ultrasensitive detection of SARS-CoV-2 spike protein by graphene field-effect transistors
Nanoscale, Vol. 15, Núm. 3, pp. 1076-1085
2021
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3D Printable Conducting and Biocompatible PEDOT-graft-PLA Copolymers by Direct Ink Writing
Macromolecular Rapid Communications, Vol. 42, Núm. 12
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Transcriptional signatures of synaptic vesicle genes define myotonic dystrophy type I neurodegeneration
Neuropathology and Applied Neurobiology, Vol. 47, Núm. 7, pp. 1092-1108
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Utrophin modulator drugs as potential therapies for Duchenne and Becker muscular dystrophies
Neuropathology and Applied Neurobiology, Vol. 47, Núm. 6, pp. 711-723
2020
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FoxO maintains a genuine muscle stem-cell quiescent state until geriatric age
Nature Cell Biology, Vol. 22, Núm. 11, pp. 1307-1318
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Genealogy of the neurodegenerative diseases based on a meta-analysis of age-stratified incidence data
Scientific Reports, Vol. 10, Núm. 1
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Myotonic Dystrophy type 1 cells display impaired metabolism and mitochondrial dysfunction that are reversed by metformin
Aging, Vol. 12, Núm. 7, pp. 6260-6275
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Neurodegeneration trajectory in pediatric and adult/late DM1: A follow-up MRI study across a decade
Annals of Clinical and Translational Neurology, Vol. 7, Núm. 10, pp. 1802-1815
2019
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COST Actions: fostering collaborative research for rare diseases
The Lancet Neurology